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Quality Capability and Risk Associate
Ver: 150
Dia de atualização: 26-11-2025
Localização: Wavre Walloon Brabant
Categoria: R & D Ciência Saúde / Assistência Médica
Indústria: Pharmaceutical Manufacturing
Tipo de empregos: Full-time
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Conteúdo do emprego
Site Name: GSK Tres Cantos, Madrid, Apollo, GSK House, Johannesburg, Munich, VeronaPosted Date: Dec 21 2022
Quality Capability & Risk Associate
The purpose of the Quality, Capability & Risk Associate (QCRA) role is to support the regional in-country QCRM team to ensure that clinical research activities are conducted by local/regional Clinical Operations staff in accordance to ICH GCP, relevant international and local regulations, requirements and guidelines, as well as GSK written standards.
Key Responsabilities
- Support the in-country QCRMs in the region with quality-related topics to ensure that clinical research activities are conducted according to ICH GCP, local legislation and GSK written standards.
- Support the development and maintenance of local plans/documentation and systems (Risk Register, Management Monitoring and Training Plan) to ensure that:
- All risks are properly managed, documented and escalated as appropriate within GSK.
- All aspects of management monitoring (MM) activities are delivered in partnership with the local Clinical Operations team, including identification and delivery of MM-related CAPAs.
- Local staff are appropriate trained to conduct their roles.
- Support issue management activities, including issue identification, resolution and escalation across all studies and local Clinical Operations teams.
- Support the implementation of ongoing quality improvement processes, including those identified during management monitoring and issue management activities.
- Support local training needs, in collaboration with the in-country QCRM, Capability Building team and local Clinical Operations Leadership Team.
- Support the in-country QCRMs to foster a quality culture and support delivery of upper quartile performance.
- Support the in-country QCRMs as the local ambassador for the global Quality, Capability and Risk Management organization.
- Work across local and regional teams to share best practices and collaborate with QCRMs and other QCRAs on ways of working.
Scientific Degree or equivalent experience ideally with some quality experience (Any science degree - e.g. life sciences, medicine, clinical research, pharmacy etc. ).
Basic Qualifications/Experience
- 3 years’ experience in Clinical Operations. Knowledge of the drug development processes and key operational interfaces.
- Good understanding of clinical/corporate governance principles
- Knowledge of ICH GCP requirements with knowledge of local and global regulatory requirements applying to Clinical Trials.
- Good written and verbal communication skills in English.
- Fluent in local language if required.
- Advanced user of MS Office (PowerPoint, Excel, Word & Outlook)
- Understanding of clinical research and the drug development process.
- Can work both independently on projects and also part of a team.
- Creative, logical, strategic thinker
- Effective problem solver and conflict resolution
- Good eye for detail and high learning agility
- Knowledge of ICH GCP / IND guidelines
- Knowledge of global and local GSK written standards.
- Understanding of the Internal Control Framework
- Act as a role model in line with GSK values and behaviors
- Collaborative and open leadership style
Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy. We’re committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce.
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GSK is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.
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Data limite: 10-01-2026
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